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RSC Advances · 2022 ·Vol. 12 ·期 54 ·35064-35071 · IF 4.036

Enhanced photocatalytic activity of a flower-like In2O3/ZnGa2O4:Cr heterojunction composite with long persisting luminescence

Ailijiang Tuerdi,Peng Yan,Fenggui He,Abdukader Abdukayum

The development of new photocatalysts with high photocatalytic efficiency and catalytic stability, and long persisting luminescence is critical for ensuring environmental protection and clean energy production. In this study, we develop a flower-like In2O3/ZnGa2O4:Cr heterojunction composite with enhanced ultraviolet (UV) photocatalytic activity using a facile two-step hydrothermal method. The spectral response range of the heterojunction composite is widened to the visible-light range owing to the presence of the ZnGa2O4:Cr persistent luminescence nanoparticles with sizes of less than 10 nm. The heterojunction composite is dispersed on the flower petals of In2O3. The In2O3/ZnGa2O4:Cr/1:1 composite exhibits photo-degradation performance for rhodamine B degradation that is superior to those of pure In2O3, ZnGa2O4:Cr, In2O3/ZnGa2O4:Cr/1:0.5 and In2O3/ZnGa2O4:Cr/1:2, achieving complete degradation after 80 min under UV light irradiation. Moreover, it exhibits long afterglow luminescence that lasts for more than 72 h. Thus, the In2O3/ZnGa2O4:Cr/1:1 composite shows great potential for use in round-the-clock photocatalytic applications.

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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2022 · IF 8.025

Iron modified chitosan/coconut shell activated carbon composite beads for Cr(VI) removal from aqueous solution

Yunquan Liu,Huimei Shan,Yanyue Pang,Hongbin Zhan,Chunya Zeng

Iron modified chitosan/coconut shell activated carbon (Fe/CSCC) composite bead is synthesized to remove Cr(VI) and is characterized to reveal the influencing factors and reaction mechanism. Results show that the adsorption capacity ( Q e ) of Cr(VI) increases with the increase of iron loading, contact time ( t ), Cr(VI) initial concentration ( C 0 ), and temperature ( T ), but decreases with the increase of pH, and mass and volume ratio ( m/v ). After 0.1 mol FeCl 3 modification, the removal efficiency of Cr(VI) by Fe/CSCC reaches as high as 97.25 % at pH = 3, m/v  = 1.0 g/L, t  = 2880 min, C 0  = 25 mg/L, and T  = 25 °C. The coexisting ions of SO 4 2− , HPO 4 − , and Ca 2+ lead to the decrease of Q e by 7.82, 5.05, and 5.50 mg/g, respectively, and the inhibition effect increases with their increasing concentrations. Fe/CSCC adsorption for Cr(VI) is an endothermic spontaneous process, and a chemical and monolayer adsorption, which is better fitted to a pseudo-second-order kinetic. The fitted maximum Q e is 64.49 mg/g by using the Langmuir model. Moreover, after five cycles of regeneration, the Q e value only drops about 3.46 mg/g. Characterization analysis of BET, XRD , FTIR , XPS, and SEM-EDS indicates that Cr(VI) is mainly adsorbed by Fe/CSCC through electrostatic attraction and complexation, which is related to the −COOH and − NH 2 groups, and Fe − O groups, respectively.

CAS / MDL: 111-30-8
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Catalysts · 2022 ·Vol. 12 ·期 11 ·1429 · IF 4.501

Study on Optimum Preparation Conditions of ZnIn2S4 to Effectively Reduce Cr(VI) under Visible Light Radiation

Yali Song,Huan Zhang,Ziyan Li,Long Huang,Junhao Xie,Long Han,Ruoying Zheng,Yuqing Zhang,Hongzhong Zhang

Previous studies have displayed various conclusions about the effect of preparation factors on the photoreduction property of ZnIn2S4. Therefore, it is not easy to figure out the optimal preparation conditions of ZnIn2S4for Cr(VI) photoreduction. To ensure Cr(VI) reduction efficiency, various ZnIn2S4photocatalysts were prepared in different solvents (i.e., water and ethylene glycol) and temperatures (i.e., 120 °C, 150 °C and 180°C). Different characterization methods were used to explain the difference in optical performance and photocatalytic property among the obtained samples. The results show that all the samples exhibit a similar band gap. The reaction solvent and temperature have a great influence on the surface morphology and optical property, leading to the different photocatalytic properties. ZnIn2S4synthesized at 120 °C in the solvothermal condition shows the optimal efficiency on Cr(VI) photoreduction due to the effective utilization of photo-induced carriers. The reasonable analysis and effective conclusion presented may provide the optimal synthesis method of ZnIn2S4to effectively remove Cr(VI) from water environment.Keywords:ZnIn2S4;Cr(VI);solvothermal;hydrothermal;photoreduction

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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

Shewanella oneidensis MR-1 for enhanced the reactivity of FA-stabilized nZVI toward Cr(VI) removal

Ling Xiong,Liying Ma,Meiqi Zhao,Haojian Zhang,Shaohua Chen

In present work, nanoscale zero-valent iron (nZVI) was successfully stabilized using fulvic acid (nZVI-FA). Shewanella oneidensis MR-1 (MR-1) was used to enhance the reactivity of the nZVI-FA. The results demonstrated that nZVI-FA combined with the MR-1 (nZVI-FA/MR-1) system could effectively solve the aggregation and surface passivation of nZVI, thereby significantly enhancing the reactivity of nZVI for   Cr(VI) removal. The Cr(VI) removal efficiency of the nZVI-FA/MR-1 system (100 %) within 24 h was apparently higher than that of the ZVI-FA system (64.43 %). The enhancement of Cr(VI) removal is because fulvic acid (FA) FA can stabilize nZVI against aggregation; MR-1 could rapidly reduce the Fe(III) (hydr)oxides (FeHOs) passivation layers on the surface of nZVI-FA to biogenic Fe(II) [bio-Fe(II)], which in turn reduced Cr(VI). X-ray photoelectron spectroscopy (XPS) analysis revealed that the Fe(II)/Fe(III) ratio (1.20) and Cr(III)/Cr(VI) ratio (2.53) of the precipitates in the nZVI-FA/MR-1 system were much higher than that those in the nZVI-FA system (0.55 and 1.40, respectively). Three-dimensional excitation-emission matrix (3D-EEM) spectral analysis confirmed that tyrosine, tryptophan, and protein-like substances in extracellular polymeric substances (EPSs) from MR-1 are vital for the removal of Cr(VI). The mechanism analysis demonstrated that most Cr(VI) was reduced to Cr(III); Cr(III) existed as Cr 2 O 3 , FeCr 2 O 4 and Cr x Fe 1-x (OH) 3 precipitates, and some of the Cr(VI) was removed from the solution by adsorption and complexation. This study offers a   low-cost, efficient, and environmentally friendly strategy to enhance the reactivity of nZVI for Cr(VI) removal, which has broad prospective applications.

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JOURNAL OF POLYMERS AND THE ENVIRONMENT · 2022 ·Vol. 31 ·期 2 ·637-647 · IF 4.705

Ultralight and Superelastic Nanofiber Aerogels with In-Situ Loaded Polypyrrole for High-Efficient Cr(VI) Adsorption

Li Dan,Liu Huipeng,Wang Ziwen,Zhang Zeqian,Wang Chengzhong,Zhao Biao,Pan Kai

Constructing 3-D nanomaterial-based adsorbents with good mechanical properties has attracted increasing attention. This paper reports a simple strategy to prepare ultralight and superelastic 3-D aerogels as efficient adsorbents for heavy metal Cr(VI) in wastewater by in-situ loading of polypyrrole on cellulose acetate nanofibers followed by freeze-drying method. The obtained aerogel possesses obvious 3-D porous and cross-linked structure, in which polypyrrole is uniformly coated on the nanofiber surface. Besides, the aerogel shows good mechanical properties with high compressive strength of 14.49 kPa, and can be processed into any desired shape. Especially, due to the presence of large specific surface area and high porosity, the obtained nanofiber aerogel shows significant Cr(VI) adsorption with maximum adsorption capacity of 244.65 mg/g. The present work proposes a high-quality nanofiber aerogel for efficiently adsorbing Cr(VI).

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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2022 ·Vol. 33 ·期 10 ·7900-7912 · IF 2.779

Hierarchical Cu2ZnSnS4 microsphere as sonocatalyst for the degradation of Rhodamine B and reduction of Cr(VI)

Hu Xuemei,Bao Jianqin,Qiao Junqiang

We report the experimental realization of using copper zinc tin sulfide (Cu 2 ZnSnS 4 ) material for sonocatalytic application for the first time. Hierarchical Cu 2 ZnSnS 4 microspheres were synthesized via a facile one-pot hydrothermal method and characterized systematically. Aggregated Cu 2 ZnSnS 4 nanosheets with an average thickness of ~ 20 nm formed a highly open hierarchical structure. The hierarchical Cu 2 ZnSnS 4 microspheres displayed remarkable sonocatalytic activity both in Rhodamine B degradation and in Cr(VI) reduction. The detailed sonocatalytic experiments revealed that Rhodamine B dye degraded up to 96.4% in 14 min and Cr(VI) reduced up to 98.7% in 10 min and both Rhodamine B degradation and Cr(VI) reduction followed pseudo-first-order kinetics. The reusability tests confirmed that the hierarchical CZTS microspheres have proper stability after 4 consecutive cycles. Moreover, the effects of initial dye concentration, various scavengers, and oxidants on the sonocatalytic RhB degradation process have also been investigated. Furthermore, the plausible mechanism of the sonocatalytic degradation in the presence of hierarchical CZTS microspheres was proposed.

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ACS Sustainable Chemistry & Engineering · 2022 · IF 9.224

Ferrocene Dicarboxylic Acid Ligand-Exchanged Hollow MIL-101(Cr) Nanospheres for Solar-Driven Atmospheric Water Harvesting

Yue Hu,Zhou Fang,Xinyi Wan,Xu Ma,Yuqi Wang,Mengyang Dong,Zhizhen Ye,Xinsheng Peng

Developing efficient water adsorbents for solar-driven atmospheric water harvesting (AWH) still remains a challenge due to the poor photothermal heating ability and slow sorption kinetics of most adsorbents. Postsynthetic ligand exchange (LE) provides an alternative strategy to prepare metal–organic framework (MOF) materials with varied structures and functions. In this work, multifunctional hollow MIL-101(Cr) with ferrocene dicarboxylic acid (Fc(COOH)2) ligand exchanged (HMF) nanospheres are prepared and utilized for efficient AWH. The resulted HMF nanospheres present great visible light absorption (>80%) and photothermal conversion ability (61.6%) due to the introduced Fc(COOH)2 ligand. The water adsorption and desorption rates of the HMF nanosorbent are 2.3 times and 4.5 times that of MIL-101(Cr). The fast water capture and solar-driven release kinetics of HMF nanosorbents indicate its great potential for actual water harvesting. The outdoor water collection experiment demonstrates that the areal water harvesting capacity of the HMF nanosorbent is 1720 g m–2 per cycle with packed thickness of 8 mm. HMF nanosorbents also demonstrate good antibacterial activity (91.4%), which is beneficial to the collection of healthy and safe water. This work provides a facile and practical method to design multifunctional MOFs from the molecular level by LE and to achieve solar-driven AWH and other fields.

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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2022 ·Vol. 29 ·期 30 ·45623-45634 · IF 5.19

Enhanced adsorptive removal of Cr(III) from the complex solution by NTA-modified magnetic mesoporous microspheres

Liang Linqing,Wang Jiahong,Tong Xinhao,Zhang Shutong

The Fe 3 O 4 @nSiO 2 @mSiO 2 /NTA (FNMs-NTA) was prepared by grafting magnetic mesoporous microspheres with nitrilotriacetic acid (NTA) and applied as an adsorbent for the removal of Cr(III) from complex solutions. Some characterization techniques including Brunauer–Emmett–Teller (BET), Fourier transform infrared spectrometer (FT-IR), X-ray diffraction (XRD), small-angle X-ray diffraction (SAXS), vibrating sample magnetometer (VSM), and thermal gravimetric analysis (TGA) were used to characterize functional groups and pore structure of FNMs-NTA, which proved that NTA was successfully decorated onto the magnetic Fe 3 O 4 @nSiO 2 @mSiO 2 (FNMs) and FNMs-NTA featured a regular mesoporous structure. The batch adsorption of Cr(III) by FNMs-NTA exhibited high adsorption capacity (16.0 mg·g −1 at pH 3.0, and 25 °C). Adsorption data followed Freundlich isotherm and adsorption process was a spontaneous adsorption process. Moreover, the kinetics of adsorption were well explained by pseudo-second-order kinetic model. FNMs-NTA showed resistance to interfering inorganic cations (Na + , Ca 2+ ) and complexing agents (EDTA). Furthermore, FNMs-NTA exhibited remarkable regeneration performance and easy separation under external magnetic field. X-ray photoelectron spectroscopy (XPS) analysis showed the FNMs-NTA had excellent adsorption ability for Cr(III) because of the ion exchange and surface complexation.

CAS / MDL: 13822-56-5
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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

Porous Cd3(C3N3S3)2/CdS composites with outstanding Cr(VI) photoreduction performance under visible light irradiation

Chumin Yan,Xiaoli Dong,Yu Wang,Nan Zheng,Hui Dang,Hongchao Ma,Xiufang Zhang

As an efficient and sustainable technology, photocatalysis driven by visible light has made great contributions to the removal of heavy metals from environment. In this work, a series of Cd 3 (TMT) 2 /CdS heterojunction composite photocatalysts were prepared by self-formation of CdS nanoparticles using an octahedral coordination polymer Cd 3 (C 3 N 3 S 3 ) 2 (denoted as Cd 3 (TMT) 2 ) as a precursor. The photocatalytic performance of Cd 3 (TMT) 2 /CdS heterojunction composites for Cr(VI) has been significantly improved under visible light irradiation owing to effective separation and migration of photoexcited charge carriers. Moreover, Cd 3 (TMT) 2 /CdS composites exhibited remarkable photocatalytic reduction performance of Cr(VI) solution with high concentration. This photocatalyst provides a novel route in the photoreduction of Cr(VI).

CAS / MDL: 7790-78-5 140-22-7
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APPLIED SURFACE SCIENCE · 2022 · IF 7.392

Synergistically enhancing electrocatalytic activity of Co2P by Cr doping and P vacancies for overall water splitting

Yu Liu,Yingying Xing,Xinyu Zheng,Shengjie Xu,Di Li,Deli Jiang

Designing high-performance and earth-abundant bifunctional catalysts for electrocatalytic water splitting remains a great challenge. Herein, a novel electrode composed of Cr-doped Co 2 P with P vacancies nanowire arrays (denoted as CrCo 2 P(V p ) NWs) grown on nickel foam was fabricated via a hydrothermal and successive calcination method. The Cr doping and vacancy engineering synergistically enable the exposure of more active sites, optimize electronic structure, and accelerate the charge transport capability, thus enhancing the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) performances. As a result, the obtained Cr 0.4 Co 2 P(V p ) NWs catalyst exhibits superior catalytic activities in 1.0 M KOH solution with low overpotentials of 37 mV at −10 mA cm −2 for HER and 253 mV at 20 mA cm −2 for OER, respectively. Furthermore, using Cr 0.4 Co 2 P(V p ) NWs as a dual-function catalyst only requires 1.54 V voltage at 10 mA cm −2 for overall water splitting. Notably, the Cr 0.4 Co 2 P(V p ) NWs catalyst displays satisfactory stability with only a small attenuation of 3.2% after 50 h in a constant current testing. This study highlights the synergistic effect between doping and anion-vacancies in the enhancement of electrocatalytic activities and provides a feasible strategy to design effective, earth-abundant, and stable bifunctional electrocatalysts for water splitting.

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Materials · 2022 ·Vol. 15 ·期 16 ·5763 · IF 3.748

Template Method for Synthesizing Hierarchically Porous MIL-101(Cr) for Efficient Removal of Large Molecular Dye

Minmin Zou,Hexin Zhu,Ming Dong,Tian Zhao

As one of the most important prototypical chromium-based MOFs, MIL-101(Cr) is well-studied and widely employed in various scientific fields. However, due to its small capture window sizes and curved internal apertures, its application in large molecular removal is quite limited, and given its high stability and high synthetic temperature (>200 °C), it is difficult to achieve hierarchically porous MIL-101(Cr). In our study, hierarchically porous MIL-101(Cr) involving a high macro-/meso-/micropores ratio was designed and synthesized using acetic acid as an additive and silicon dioxide (SiO2) nanoparticles as a template. The optimal hierarchically porous MIL-101(Cr) (A-4) possessed a high specific surface area (2693 m2g−1) and an abundant macro-/mesoporous structure with the addition of SiO2of 200 mg. Compared with the control sample (A-0) with a less macro-/mesoporous structure, A-4 showed good adsorption properties for both coomassie brilliant blue R-250 (CBB, 82.1 mg g−1) and methylene blue (MB, 34.3 mg g−1) dyes, which were 1.36 times and 9.37 times higher than those of A-0. Moreover, A-4 also had good recyclability, and the removal rate of CBB was still higher than 85% after five cycles of adsorption.Keywords:MIL-101(Cr);SiO2;dye adsorption;template

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Nanomaterials · 2022 ·Vol. 12 ·期 11 ·1846 · IF 5.719

Marine Biomass-Supported Nano Zero-Valent Iron for Cr(VI) Removal: A Response Surface Methodology Study

Zhuang Tong,Qin Deng,Shengxu Luo,Jinying Li,Yong Liu

Heavy metal ions such as Cr(VI) pose great hazards to the environment, which requests materials and methods for decontamination. Nano zero-valent iron (nZVI) has emerged as a promising candidate for Cr(VI) removal. Herein, harnessing the merits of marine biomass, a heterogeneous water treatment system for the decontamination of Cr(VI) is developed based on the in situ immobilization of nZVI on the seashell powder (SP)-derived porous support. A response surface methodology (RSM) study involving three independent factors is designed and conducted to direct material synthesis and reaction design for products with optimal performances. Under optimal synthetic conditions, the nZVI-loaded seashell powder (SP@nZVI), which is characterized in detail by scanning electron microscope (SEM), X-ray diffraction (XRD), and Fourier-transform infrared spectroscopy (FTIR), results in a 79% increase in the removal efficiency of Cr(VI) compared to free nZVI. Mechanism studies show that the removal of Cr(VI) by SP@nZVI conforms to the Langmuir adsorption model with a quasi-second order kinetic equation, in which redox reactions between nZVI and Cr(VI) occurred at the SP surface. The results of this work are expected to benefit the reuse of bioresource waste in developing environmental remediation materials.Keywords:seashell resource utilization;pyrolysis;zero-valent iron;response surface methodology;chromium removal

CAS / MDL: 13478-10-9
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